Medical Device Recalls
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1 result found
510(K) Number: K200696 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model/Catalog Numb... | 3 | 12/11/2025 | Orthofix U.S. LLC |
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